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HEARTPORT ENDOPULMONARY VENT CATHETER

Page Type
Cleared 510(K)
510(k) Number
K981009
510(k) Type
Traditional
Applicant
HEARTPORT, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/4/1998
Days to Decision
170 days
Submission Type
Summary

HEARTPORT ENDOPULMONARY VENT CATHETER

Page Type
Cleared 510(K)
510(k) Number
K981009
510(k) Type
Traditional
Applicant
HEARTPORT, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/4/1998
Days to Decision
170 days
Submission Type
Summary